FDA.reportPublic FDA data

Sunscreen Glowing

Manufacturer
Aopline Health Industry Technology (Guangzhou) Co., Ltd.
Effective date
2024-12-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:41:15

Label at a glance#

ProductSunscreen Glowing
Active ingredientAVOBENZONE, OCTISALATE, HOMOSALATE, OCTOCRYLENE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE G63QQF2NOX 3.0%
OCTISALATE 4X49Y0596W 5.0%
OCTOCRYLENE 5A68WGF6WM 7.0%
HOMOSALATE V06SV4M95S 9%

OTC - PURPOSE SECTION

Sunscreen

OTC - DO NOT USE SECTION


For external use only Do not use on damaged !i or broken skin.
When using this product keep out of eyes.Rise with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. lf swallowed, get medical help or contact a Poison ControlCenter right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison ControlCenter right away

OTC - STOP USE SECTION


When using this product keep out of eyes.
Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

OTC - WHEN USING SECTION


Directions
Apply liberally 15 minutes before sun exposure. Reapply: at least every 2 hours or after 80 minutes of swimming or sweating. Sun Protection Measures: $pending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPfof 15 or higher and other sun protection measures including: limit time in the sun, especiallyfrom 10 a.m.-2 pm, and wear long-sleeved shirts, pants, hats, and sunglasses. Childrenunder 6 months of age ask a doctor.

INACTIVE INGREDIENT SECTION

WATER
BUTYLOCTYL SALICYLATE
NEOPENTYL GLYCOL DIHEPTANOATE
MICA
CI 77891
BUTYL METHOXYDIBENZOYLMETHANE
GLYCERIN
PROPYLENE GLYCOL
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER
CETEARYL ALCOHOL
COCO-GLUCOSIDE
GLYCERYL STEARATE
PEG-100 STEARATE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
SILICA
POTASSIUM CETYL PHOSPHATE
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
CETEARYL ALCOHOL
HYDROXYACETOPHENONE
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
CI 77492
TRIETHOXYCAPRYLYLSILANE
DISODIUM EDTA
CI 77491
CI 77499

INDICATIONS & USAGE SECTION


Uses

Helps prevent sunburn.lf used as directed with other sun protection measures (see Directions), decreases therisk of skin cancer and early skin aging causedby the sun.

WARNINGS SECTION


For external use only. Do not use on damagedor broken skin.
When using this product keep out of eyes.nse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. lf swallowed, get medical help or contact a Poison ControlCenter right away

DOSAGE & ADMINISTRATION SECTION


Apply liberally 15 minutes before sun exposure.

Reapply: at least every 2 hours or after 80 minutes of swimming or sweating.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELINGPACKAGE LABELING

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82723-010-012026-01-29C16284748780-149896155-9fee-586f-e063-e6dba90add9028c2795d-0351-13c8-e063-6394a90a56d7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82723-010-01Sunscreen Glowing60 mL in 1 BOTTLELOTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82723-010SUNSCREEN GLOWING (SUNSCREEN GLOWING LOTION) LOTION [AOPLINE HEALTH INDUSTRY TECHNOLOGY (GUANGZHOU) CO., LTD.]11 package rows20241209_28c2795d-0351-13c8-e063-6394a90a56d7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82723-01082723-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
MICAV8A1AW0880IACT
CI 77499XM0M87F357IACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)H895X08VNQIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CI 774911K09F3G675IACT
GLYCERINPDC6A3C0OXIACT
PEG-100 STEARATEYD01N1999RIACT
CI 7789115FIX9V2JPIACT
COCO GLUCOSIDEICS790225BIACT
GLYCERYL STEARATE230OU9XXE4IACT
OCTOCRYLENE5A68WGF6WMACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
CETEARYL ALCOHOL2DMT128M1SIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
CI 77492EX438O2MRTIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SILICAETJ7Z6XBU4IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
28c2795d-0352-13c8-e063-6394a90a56d728c2795d-0351-13c8-e063-6394a90a56d72024-12-08WarningsExact identifier
spl id: 28c2795d-0352-13c8-e063-6394a90a56d7
spl set id: 28c2795d-0351-13c8-e063-6394a90a56d7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.